Telecommute – Istanbul, Turkey
STATISTICAL PROGRAMMER II – Turkey (home based)
Istanbul, Turkey (QIST, Home-based)
IQVIA? is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
Real World Evidence Programmers. Exciting new solution-driven roles based at home.
IQVIA’s Real World Evidence Solutions group is recruiting Programmers to join our dynamic team in Europe.
The RWE Programming roles will provide statistical programming expertise, informing data harmonization for primary data and secondary data from multiple sources (EMRs, PROs, eCRF, Observational studies, etc.) advise on database design and data collection, and the programming of tables, listings and figures using SAS (Base SAS, SAS/STAT and SAS Macro) and other applications. These are exciting new solution-driven roles within the team as RWES expands into developing further innovations for clients.
Work independently when required
Act as technical lead from time to time
Perform planning activity from time to time
Report directly to both external and internal clients
Develops, executes and reviews programs to provide statistical programming support for statisticians, clients, or business demands to source, organize (creating statistical tables, listings, and graphs) and interpret complex data sets.
Conducts statistical analyses for client reports and publications and utilize findings, and insights for practical application to further business operations, come across innovative findings and discoveries for solution and product development
Perform the programming quality control checks for the source data and report data issues periodically
Detect errors in detail and correct. e.g., review tables/listings, edit checks output and SAS programs to ensure quality of deliverables
Assist in the development of programming documentation including specifications, as appropriate, under supervision
Provide advanced technical expertise in conjunction with internal and external clients, and bring project solutions to teams and department, under supervision
Develop, implement and validate new process technologies, macros and applications under supervision
Fulfil project responsibilities at the level of assisting the statistical programming team lead
Understand timelines for and milestones affecting their work and alert supervisor to potential slippage
MINIMUM SKILLS, EXPERIENCE & QUALIFICATIONS FOR STAT PROG II:
Knowledge of statistics, programming and/or clinical drug development process
Working knowledge of computing applications such as Base SAS, SAS/STAT and SAS Macro Language
Working knowledge of the SDTM structure
2 years working knowledge of the ADaM standards in clinical trials
2 years working knowledge of TLFs in clinical trials
In-depth knowledge of applicable clinical research regulatory requirements would be an advantage; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Ability to implement programming specifications as appropriate
Ability to estimate programming scope of work and assist in communicating project status
Able to solve complex probl…
Statistics,Math & Economics,Medical & Health,Medical Research